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Mini Oral session: Non-metastatic NSCLC and other thoracic malignancies

LBA50 - Analysis of pathological features and efficacy outcomes with neoadjuvant nivolumab (N) plus platinum-doublet chemotherapy (C) for resectable non-small cell lung cancer (NSCLC) in CheckMate 816

Date

12 Sep 2022

Session

Mini Oral session: Non-metastatic NSCLC and other thoracic malignancies

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Janis Taube

Citation

Annals of Oncology (2022) 33 (suppl_7): S808-S869. 10.1016/annonc/annonc1089

Authors

J.S. Deutsch1, A. Cimino-Mathews2, E.D. Thompson2, D. Wang3, R.A. Anders2, E. Gabrielson2, P. Illei2, J. Jedrych3, L. Danilova4, J. Spicer5, M. Provencio Pulla6, P.M. Forde7, D. Pandya8, M.P. Tran9, J. Fiore10, V. Devas11, T.R. Cottrell2, A.S. Baras12, J.M. Taube13

Author affiliations

  • 1 Pathology Department, Johns Hopkins University SOM, 21287 - Baltimore/US
  • 2 Pathology, Johns Hopkins University SOM, Baltimore/US
  • 3 Dermatology, Johns Hopkins University SOM, Baltimore/US
  • 4 Division Of Biostatistics And Bioinformatics, Johns Hopkins University SOM, Baltimore/US
  • 5 Thoracic Oncology, McGill University Health Centre, H3A 1X1 - Montreal/CA
  • 6 Medical Oncology, Hospital Universitario Puerta de Hierro, Madrid/ES
  • 7 Thoracic Oncology, Bloomberg-Kimmel Institute for Cancer Immunotherapy, Baltimore/US
  • 8 Pathology, Bristol Myers Squibb, 08648 - Princeton/US
  • 9 Ww Medical Oncology , Bristol Myers Squibb, Princeton/US
  • 10 Oncology Clinical Development, Bristol Myers Squibb, 08640 - Princeton/US
  • 11 Global Biometrics And Data Science, Bristol Myers Squibb, 08648 - Princeton/US
  • 12 Pathology Informatics, Johns Hopkins University SOM, Baltimore/US
  • 13 Dermatopathology, Johns Hopkins University SOM, 21287 - Baltimore/US

Resources

This content is available to ESMO members and event participants.

Abstract LBA50

Background

A post hoc analysis from the phase 3 CheckMate 816 study showed that residual viable tumor (RVT) in the primary tumor (PT) was associated with event-free survival (EFS) with N + C (2y EFS rates: 90%, 60%, 57%, and 39% in patients [pts] with 0–5, > 5–30, > 30–80, and > 80% RVT). Here, we report analyses in pts with or without (w/o) pathologic evidence of lymph node involvement (LN-I).

Methods

Adults with resectable NSCLC were randomized to receive N 360 mg + platinum-doublet C Q3W or C alone Q3W for 3 cycles, followed by resection. Primary endpoints were pathologic complete response (pCR) and EFS (both met). Analyses included efficacy by LN-I and assessment of prespecified histopathologic features (%RVT, regression, and necrosis) in PT and LN. Pts with LN-I could have had either 0% (pathologic evidence of completely regressed tumor) or > 0%RVT in the resected LN. A time-dependent ROC curve analysis assessed the predictive ability of %RVT in PT for 2y EFS.

Results

pCR rates were improved with N + C vs C in both pts with or w/o LN-I (table); similar EFS benefit was seen in pts with or w/o LN-I (HR: 0.69 and 0.74). In the N + C arm, pts with LN-I who had 0% RVT in both PT and LN showed the best EFS outcomes numerically, followed by those with 0% RVT in either PT or LN; those with > 0% RVT in both PT and LN showed shorter EFS (2y EFS rates: 92%, 76%, and 49%). Overall, lower %RVT and higher % regression (appears to be inversely related to RVT) was seen with N + C vs C in PT and LN; % necrosis did not differ between the treatment arms (table). In both pts with or w/o LN-I (N + C), %RVT in PT was predictive of EFS at 2y (AUC: 0.76 and 0.73).

Conclusions

These findings further support neoadjuvant N + C vs C as a novel treatment option for pts with resectable NSCLC, regardless of LN-I. %RVT in PT in pts with or w/o LN-I was associated with EFS with N + C. Further assessment of clinically relevant %RVT cutoffs to predict long-term outcomes with immunotherapy is warranted. Table: 000LBA50

Path-evaluable a
W/o LN-I With LN-I
N + C (n = 72) C (n = 51) N + C (n = 68) C (n = 74)
Efficacy
Median EFS (95% CI), mo NR (30.6–NR) NR (22.4–NR) 31.6 (22.2–NR) 22.7 (14.8–NR)
EFS HR (95% CI) 0.74 (0.39–1.41) 0.69 (0.42–1.13)
pCR, % 0% RVT, PT 0% RVT, LN 0% RVT, PT and LN 0% RVT, PT or LN 40 – – – 6 – – – 24 34 19 38 3 5 1 7
Path features, median (Q1–Q3)
%RVT PT LN 1 (0–48) – 65 (12–90) – 35 (2–82) 40 (0–100) 82 (50–94) 96 (61–100)
% Regression PT LN 80 (18–99) – 20 (4–70) – 40 (6–82) 20 (0–85) 13 (4–44) 1 (0–15)
% Necrosis PT LN 4 (0–18) – 2 (0–10) – 1 (0–16) 0 (0–15) 1 (0–6) 0 (0–2)

a140 (78%) and 125 (70%) of concurrently randomized pts in N + C and C arms had path-evaluable samples from both PT and LN. NR, not reached.

Clinical trial identification

NCT02998528.

Editorial acknowledgement

Editorial assistance in the writing of the abstract was provided by Wendy Sacks, PhD, and Michele Salernitano of Ashfield MedComms, an Inizio company.

Legal entity responsible for the study

Bristol Myers Squibb.

Funding

Bristol Myers Squibb.

Disclosure

J.S. Deutsch: Financial Interests, Personal, Other, Application No: 63/313,548: Patent pending. A. Cimino-Mathews: Financial Interests, Personal, Advisory Role: Bristol Myers Squibb; Financial Interests, Institutional, Funding, Research funding to institution: Bristol Myers Squibb. D. Wang: Financial Interests, Personal, Full or part-time Employment: Akoya Biosciences. P. Illei: Financial Interests, Personal, Advisory Board, Pathology advisory board on NSCLC biomarker testing: AstraZeneca, Bristol Myers Squibb, Janssen, Roche; Financial Interests, Personal, Invited Speaker, Unbranded education on NSCLC biomarker testing: Eli Lilly, Genentech; Financial Interests, Personal, Stocks/Shares, 100 SHARES: Bristol Myers Squibb; Non-Financial Interests, Institutional, Other, Co-PI on an institutional grant (central pathology review): Bristol Myers Squibb; Non-Financial Interests, Institutional, Other, Co-PI: Erbe GmBH. J. Spicer: Financial Interests, Personal, Other, speaker, consultancy, advisory role: Merck, BMS, Roche, AstraZeneca, Protalix Biotherapeutics, Chemocentryx; Financial Interests, Personal, Funding, Research funding: Merck, Roche, Protalix Biotherapeutics, CLS Therapeutics; Non-Financial Interests, Personal, Proprietary Information: AstraZeneca, Protalix Biotherapeutics, CLS Therapeutics. M. Provencio Pulla: Financial Interests, Personal, Advisory Board: BMS, MSD, Bayer, Lilly, Roche, Takeda, Janssen; Non-Financial Interests, Leadership Role, President of Spanish Lung cancer Group: President; Non-Financial Interests, Leadership Role, Insutituto Investigación Sanitaria Puerta de Hierro: Director. P.M. Forde: Financial Interests, Personal, Advisory Board: Amgen, AstraZeneca, BMS, Daiichi, F-Star, G1, Genentech, Iteos, Janssen, Merck, Novartis, Sanofi, Surface; Financial Interests, Institutional, Funding, Research funding to institution: AstraZeneca, BioNTech, BMS, Corvus, Kyowa, Novartis, Regeneron ; Financial Interests, Personal, Other, Trial steering committee membership: AstraZeneca, Biontech, BMS, Corvus; Non-Financial Interests, Personal, Member of the Board of Directors: Mesothelioma Applied Research Foundation; Non-Financial Interests, Personal, Advisory Board: LUNGevity. D. Pandya: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks/Shares: Bristol Myers Squibb. M.P. Tran: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks/Shares: Bristol Myers Squibb. J. Fiore: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks/Shares: Bristol Myers Squibb. V. Devas: Financial Interests, Personal, Full or part-time Employment: Bristol Myers Squibb; Financial Interests, Personal, Stocks/Shares: Bristol Myers Squibb. J.M. Taube: Financial Interests, Personal, Advisory Board: Bristol Myers Squibb, Merck, AstraZeneca, Genentech, Akoya Biosciences, Lunaphore Technologies, Compugen; Financial Interests, Personal, Stocks/Shares: Akoya Biosciences; Financial Interests, Institutional, Funding, Research funding to institution: Bristol Myers Squibb, Akoya Biosciences; Non-Financial Interests, Personal, Other, Equipment loan and reagent provision: Akoya Biosciences; Other, Personal, Invited Speaker, Patent pending for machine learning for irPRC scoring: Akoya Biosciences. All other authors have declared no conflicts of interest.

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